These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

162 related items for PubMed ID: 7422065

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. A 45,XX,-5,-14,+t(5q;14q)mat cri du chat child.
    Bass HN, Sparkes RS, Crandall BF, Galos KJ, Howard J.
    Ann Genet; 1978 Mar; 21(1):56-9. PubMed ID: 308345
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome.
    Goodart SA, Simmons AD, Grady D, Rojas K, Moyzis RK, Lovett M, Overhauser J.
    Genomics; 1994 Nov 01; 24(1):63-8. PubMed ID: 7896290
    [Abstract] [Full Text] [Related]

  • 5. [Cri-du-chat syndrome. A case report].
    Diop IB, Sy Signate H, Ba SA, Sarr M, Hane L, Diame H, Kane A, Dieye O, Sow D, Diouf SM, Fall M.
    Dakar Med; 2000 Nov 01; 45(1):95-7. PubMed ID: 14666800
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Familial occurrence of the cat's cry (cri du chat) syndrom resulting from a balanced t(5 : 12) translocation (author's transl)].
    Mazurczak T, Stolarska A, Sito A, Mataszewska K.
    Probl Med Wieku Rozwoj; 1977 Nov 01; 7():169-77. PubMed ID: 614567
    [No Abstract] [Full Text] [Related]

  • 11. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D, Boccone L, Ristaldi MS, Nucaro AL.
    Genet Couns; 2008 Nov 01; 19(4):381-6. PubMed ID: 19239081
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Partial B trisomy in cat-cry-syndrome (author's transl)].
    Schwingshackl A, Ganner E.
    Padiatr Padol; 1973 Nov 01; 8(4):362-71. PubMed ID: 4745566
    [No Abstract] [Full Text] [Related]

  • 16. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson EC, Holden JJ, Lewis ME, Rajcan-Separovic E.
    Clin Genet; 2005 Apr 01; 67(4):341-51. PubMed ID: 15733271
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.
    Laczmanska I, Stembalska A, Gil J, Czemarmazowicz H, Sasiadek M.
    Eur J Med Genet; 2006 Apr 01; 49(1):87-92. PubMed ID: 16473315
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.